Senior Manufacturing Supervisor, Shift (Biopharma)

  • Location

    Singapore

  • Sector:

    Engineering & Manufacturing

  • Job type:

    Permanent

  • Salary:

    S$5000 - S$8000 per month + Shift allowance + transportation allowance

  • Contact:

    Abhik Damani

  • Contact email:

    abhik.damani@voltasia.com.sg

  • Job ref:

    BBBH8040_1584587465

  • Published:

    about 4 years ago

  • Expiry date:

    2020-04-18

  • Consultant:

    ConsultantDrop

My client is a world player in the biopharma industry and are on the lookout for a Senior Manufacturing Supervisor (shift) to lead their entire floor operations.

Responsibilities

  • Responsible for the hands-on, daily supervision of GMP manufacturing operations and personnel within the manufacturing site
  • Participate in all aspects of personnel management (interviewing, training, coaching and developing).
  • Responsible for all day to day operations in the GMP manufacturing site, as assigned.
  • Specific responsibilities will include
    • Hands on supervision and support of manufacturing staff
    • Write and revise batch records, SOPs and solution preparation documents to ensure compliance to GMPs
    • Timely review of completed manufacturing documentation (batch records, worksheets, solution docs., etc
    • Schedule manufacturing staff to ensure manufacturing timelines are met
    • Review production schedule and priorities to establish shift assignments.
    • Ensure required levels of safety, quality and productivity are met.
    • Work effectively within the management team to execute goals, objectives and tasks to achieve desired results.
    • Aid in problem solving manufacturing process issues
    • Timely reporting, investigation and resolution of manufacturing deviations.
    • Serve as lead trainer on manufacturing processes and all related equipment.
    • Provide cross-functional coordination and issue resolution.
  • Comply with Safety, Health & Environmental (SHE) requirements,
  • Collaborate with cross-functional teams (i.e. QA/QC, F&E, PPIC, Mfg. PD, Regulatory, etc.) in completing production activities
  • Oversees set up of critical manufacturing processes and ensure responsibility for resolving all problems during operations
  • Ensure aseptic techniques training programs are maintained and constantly improved

Requirements:

  • Degree in Life Sciences/Biotechnology/Engineering or equivalent
  • At least 7 years' experience in a biopharma environment with 3-5 years in a supervisory role
  • Strong Knowledge of GMP systems
  • Demonstrated ability to trouble shoot process and equipment problems with good problem-solving skills
  • Ability to work in a 12-hour rotating shift

Please send your resume in WORD format by clicking the apply button below or contact Abhik Damani on +65 6701 1527 for a confidential discussion. Please note that only short-listed candidates will be contacted. CEI Reg. Number R1544061 (Abhik Damani).